Rappel de Device Recall Dimension Vista Intelligent Lab Systems

Selon U.S. Food and Drug Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à United States qui a été fabriqué par Siemens Healthcare Diagnostics, Inc..

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
  • ID de l'événement
  • Classe de risque de l'événement
    Class 2
  • Numéro de l'événement
  • Date de mise en oeuvre de l'événement
  • Date de publication de l'événement
  • Statut de l'événement
  • Pays de l'événement
  • Date de fin de l'événement
  • Source de l'événement
  • URL de la source de l'événement
  • Notes / Alertes
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Notes supplémentaires dans les données
    Analyzer, chemistry (photometric, discrete), for clinical use - Product Code JJE
  • Cause
    Siemens is conducting a field correction for dimension vista 500 and dimension vista 1500 systems using software versions 3.5.1 and 3.6. under specific rare conditions which require a system reset, there is a potential for a sample to be dispensed into an aliquot well that has previously been used for a qc or calibrator product from a vista vial. if two samples are dispensed into the same aliquot.
  • Action
    The firm, Siemens, sent an "Urgent Medical Device Correction" letter dated June 2013 to its consignees/customers. The letter describes the product, problem and actions to be taken. The customers were instructed to take the following actions: 1) In the event that an instrument Reset is required for any reason, review the Current Activities Screen to determine if there are any pending QC or Calibration tests. 2) If there are no pending QC of Calibration tests, Rest the instrument or troubleshoot the instrument per the Operators Guide. 3) If there are pending QC or Calibration tests, restarting the software is necessary before resuming patient processing. Go to Operation -> Shutdown, confirm Yes, then on the blue console menu screen select start Vista. Consignees/customers were also asked to complete the Field Effectiveness Check form attached to the letter via fax to Siemens Healthcare Diagnostics at (302) 621-8467, and retain the letter with laboratory records, and forward the letter to those who may have received the product. If you have any questions, contact your Siemens Customer Care Center at (800-441-9250)-Technical Solutions or your local Siemens Technical Support representative.


  • Modèle / numéro de série
    Dimension Vista 500 Siemens material numbers: 10284473 (domestic), and 10488224 (international), Dimension Vista 1500 Siemens material numbers: 10444801 (domestic) and 10444802 (international).
  • Classification du dispositif
  • Classe de dispositif
  • Dispositif implanté ?
  • Distribution
    Worldwide distribution: US (nationwide) including PR and countries of: Australia, Austria, Belgium, Canada, Czech Republic, Denmark, Finland, France, Germany, Italy, Japan, Malaysia, Netherlands, New Zealand, Norway, Portugal, Republic Korea, Saudia Arabia, Slovakia, Slovenia, South Africa, Spain, Switzerland, and United Kingdom.
  • Description du dispositif
    Dimension Vista 500 and Dimension Vista 1500 System Aliquot Well Double Dispense with software versions 3.5.1 and 3.6. || In vitro diagnostic device intended to duplicate manual analytical procedures such as pipetting, mixing, heating, and measuring spectral intensities to determine a variety of analytes in human body fluids. Dimension Vista chemical and immunochemical applications use photometric, turbidimetric, chemiluminescence, nephelometric, and integrated ion-selective multisensory technology for clinical use.
  • Manufacturer


  • Adresse du fabricant
    Siemens Healthcare Diagnostics, Inc., 500 Gbc Dr Ms 514, PO BOX 6101, Newark DE 19702-2466
  • Société-mère du fabricant (2017)
  • Source